Ventus Medical, Inc.

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Web: http://www.ventusmedical.com
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Address: 1301 Shoreway Rd., Ste 340, Belmont, California 94002, USA
Phone: +1-(650)-632.4199 | Fax: +1-(650)-632.4198 | Map/Directions >>

Profile: Ventus Medical, Inc. has developed Provent® a breakthrough sleep apnea therapy for patients with obstructive sleep apnea.

5 Products/Services (Click for related suppliers)

• For Obstructive Sleep Apnea Intranasal Expiratory Resistance Valve (FDA Code: OHP / 872.5570)

Intraoral devices for snoring and intraoral devices for snoring and obstructive sleep apnea are devices that are worn during sleep to reduce the incidence of snoring and to treat obstructive sleep apnea. The devices are designed to increase the patency of the airway and to decrease air turbulence and airway obstruction. The classification includes palatal lifting devices, tongue retaining devices, and mandibular repositioning devices.

• Nasal Dilator (FDA Code: LWF / 874.3900)

A nasal dilator is a device intended to provide temporary relief from transient causes of breathing difficulties resulting from structural abnormalities and/or transient causes of nasal congestion associated with reduced nasal airflow. The device decreases airway resistance and increases nasal airflow. The external nasal dilator is constructed from one or more layers of material upon which a spring material is attached, with a skin adhesive applied to adhere to the skin of the nose; it acts with a pulling action to open the nares. The internal nasal dilator is constructed from metal or plastic and is placed inside the nostrils; it acts by pushing the nostrils open or by gently pressing on the columella.

• Obstructive Sleep Apnea (OSA) Treatment

• Sleep Apnea Equipment

• Ventilatory Effort Recorder (FDA Code: MNR / 868.2375)

A breathing (ventilatory) frequency monitor is a device intended to measure or monitor a patient's respiratory rate. The device may provide an audible or visible alarm when the respiratory rate, averaged over time, is outside operator settable alarm limits. This device does not include the apnea monitor classified in 868.2377.